CAS 3066-90-8
:2,3-Dimethoxy-5-methyl-1,4-benzenediol
Description:
2,3-Dimethoxy-5-methyl-1,4-benzenediol, with the CAS number 3066-90-8, is an organic compound characterized by its aromatic structure featuring a benzene ring substituted with two methoxy groups and a methyl group, along with two hydroxyl groups. This compound is a derivative of catechol, which contributes to its potential antioxidant properties. It typically appears as a solid at room temperature and is soluble in organic solvents due to the presence of methoxy groups, which enhance its hydrophobic character. The hydroxyl groups can participate in hydrogen bonding, influencing its reactivity and solubility in polar solvents. 2,3-Dimethoxy-5-methyl-1,4-benzenediol may exhibit biological activity, making it of interest in various fields, including pharmaceuticals and materials science. Its synthesis often involves the methylation of catechol derivatives, and it can be analyzed using techniques such as NMR and mass spectrometry to confirm its structure and purity. As with many organic compounds, safety precautions should be taken when handling it in laboratory settings.
Formula:C9H12O4
InChI:InChI=1S/C9H12O4/c1-5-4-6(10)8(12-2)9(13-3)7(5)11/h4,10-11H,1-3H3
InChI key:InChIKey=DSBZYDDWLLIJJS-UHFFFAOYSA-N
SMILES:O(C)C1=C(OC)C(O)=C(C)C=C1O
Synonyms:- 1,4-Benzenediol, 2,3-dimethoxy-5-methyl-
- 2,3-Dimethoxy-5-Methylbenzene-1,4-Diol
- 2,3-Dimethoxy-5-methyl-1,4-benzenediol
- 2,3-Dimethoxy-5-methyl-1,4-benzohydroquinone
- 2,3-Dimethoxy-5-methyl-1,4-dihydroxybenzene
- 2,3-Dimethoxy-5-methylbenzohydroquinone
- 2,3-Dimethoxy-5-methylhydroquinone
- Coenzyme Q<sub>0</sub>, dihydro-
- Hydroquinone, 2,3-dimethoxy-5-methyl-
- Reduced coenzyme Q<sub>0</sub>
- Ubiquinol 0
- Coenzyme Q0, dihydro-
- See more synonyms
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Found 7 products.
1,4-Benzenediol, 2,3-dimethoxy-5-methyl-
CAS:Formula:C9H12O4Purity:98%Color and Shape:SolidMolecular weight:184.18922,3-Dimethoxy-5-methylhydroquinone
CAS:<p>2,3-Dimethoxy-5-methylhydroquinone</p>Purity:98%Molecular weight:184.19g/mol2,3-Dimethoxy-5-methyl-1,4-hydroquinone
CAS:<p>2,3-Dimethoxy-5-methyl-1,4-hydroquinone is an organic compound belonging to the class of hydroquinones, which is a type of phenolic antioxidant. It is synthesized through chemical reactions involving methoxylation and methylation of hydroquinone precursors. This compound acts primarily as an electron donor, efficiently reducing reactive oxygen species (ROS) and stabilizing free radicals by donating electrons, thereby exhibiting potent antioxidant activity.</p>Formula:C9H12O4Purity:Min. 95%Color and Shape:PowderMolecular weight:184.19 g/mol2,3-Dimethoxy-5-methylhydroquinone
CAS:Formula:C9H12O4Purity:98%Color and Shape:SolidMolecular weight:184.1912,3-Dimethoxy-5-methyl-1,4-hydroquinone
CAS:Controlled Product<p>Stability Light Sensitive<br>Applications A substituted p-hydroquinone derivative with antioxidant properties and inhibitory effects in lipid peroxidation. It is a free radical scavenger that can potentially be modified to suppress hydrogen peroxide-induced cytotoxicity and DNA damage in relation to affinity for cell membrane.<br>References Roginsky, V. et al.: Chem. Phys. Lipids, 125, 49 (2003); Nakayama, T.: Food. Fact. Cancer Prev., 642 (1997);<br></p>Formula:C9H12O4Color and Shape:NeatMolecular weight:184.19






